PMA P000018S022
- Device
- NOVOSTE/BETA-CATH SYSTEM
- Applicant
- Best Vascular, Inc.
- PMA number
- P000018
- Supplement
- S022
- Product code
- MOU
- Decision date
- 2002-06-28
- Classification
- Intravascular Radiation Delivery System
- Generic name
- Intravascular radiation delivery system
- Approval order statement
- CHANGE IN THE MANUFACTURING PROCESS TO ELIMINATE AN INSPECTION TEST.
Current openFDA PMA Record#
- Device
- NOVOSTE/BETA-CATH SYSTEM
- Applicant
- Best Vascular, Inc.
- PMA number
- P000018
- Supplement
- S022
- Product code
- MOU
- Generic name
- Intravascular radiation delivery system
- Decision date
- 2002-06-28
- Decision code
- OK30
- Date received
- 2002-06-06
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGE IN THE MANUFACTURING PROCESS TO ELIMINATE AN INSPECTION TEST.